Variant (rsID / SNP)

rs11465553

rs11465553 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to IL17F. Location: chromosome 6, position 52,101,758. Clinical significance in the table: Benign.

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Reference-table entries

IL17FBenign

Clinical significance (as recorded): Benign
Variant type: single nucleotide variant
Chromosome / position: 6:52101758
Cytoband: 6p12.2
HGVS: NM_052872.4(IL17F):c.463G>A (p.Val155Ile)
Allele change: Missense_V155I

Associated conditions / phenotypes

Candidiasis, familial, 6

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.